BR0308091A - Processes for the synthesis of 5'-deoxy-5'-chloroadenosine and 5'-deoxy-5'-methylthioadenosine - Google Patents

Processes for the synthesis of 5'-deoxy-5'-chloroadenosine and 5'-deoxy-5'-methylthioadenosine

Info

Publication number
BR0308091A
BR0308091A BR0308091-9A BR0308091A BR0308091A BR 0308091 A BR0308091 A BR 0308091A BR 0308091 A BR0308091 A BR 0308091A BR 0308091 A BR0308091 A BR 0308091A
Authority
BR
Brazil
Prior art keywords
chloroadenosine
deoxy
synthesis
methylthioadenosine
processes
Prior art date
Application number
BR0308091-9A
Other languages
Portuguese (pt)
Inventor
James Edward Saenz
Jayaram Kasturi Srirangan
Original Assignee
Pfizer
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Pfizer filed Critical Pfizer
Publication of BR0308091A publication Critical patent/BR0308091A/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H19/00Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
    • C07H19/02Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
    • C07H19/04Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
    • C07H19/16Purine radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H19/00Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
    • C07H19/02Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
    • C07H19/04Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
    • C07H19/16Purine radicals
    • C07H19/173Purine radicals with 2-deoxyribosyl as the saccharide radical
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C1/00Making non-ferrous alloys
    • C22C1/08Alloys with open or closed pores
    • C22C1/083Foaming process in molten metal other than by powder metallurgy
    • C22C1/086Gas foaming process

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Biotechnology (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Molecular Biology (AREA)
  • Metallurgy (AREA)
  • Mechanical Engineering (AREA)
  • Materials Engineering (AREA)
  • Saccharide Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

"PROCESSOS PARA A SìNTESE DE 5<39>-DESóXI-5<39>CLOROADENOSINA E 5<39>-DESóXI-5<39>-METILTIOADENOSINA". A presente invenção refere-se a um processo para preparar in situ cloroadenosina, em que adenosina em um solvente não-aquoso é feita reagir com um cloreto de tionila e uma piridina para formar uma solução reacional; o solvente não-aquoso é trocado por um álcool inferior, e é adicionada uma base à solução reacional; e a cloroadenosina resultante é filtrada, lavada e seca. Adicionalmente, é descrito um processo em duas etapas para a síntese de metiltioadenosina utilizando a cloroadenosina preparada in situ."PROCESSES FOR THE SYNTHESIS OF 5 <39> -DESOXY-5 <39> CHLOROADENOSIN AND 5 <39> -DESOXY-5 <39> -METHYLTHYOADENOSINE". The present invention relates to a process for preparing chloroadenosine in situ, wherein adenosine in a non-aqueous solvent is reacted with a thionyl chloride and a pyridine to form a reaction solution; the non-aqueous solvent is exchanged for a lower alcohol, and a base is added to the reaction solution; and the resulting chloroadenosine is filtered, washed and dried. Additionally, a two-step process for the synthesis of methylthioadenosine using chloroadenosine prepared in situ is described.

BR0308091-9A 2002-03-04 2003-02-17 Processes for the synthesis of 5'-deoxy-5'-chloroadenosine and 5'-deoxy-5'-methylthioadenosine BR0308091A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US36128402P 2002-03-04 2002-03-04
PCT/IB2003/000595 WO2003074541A1 (en) 2002-03-04 2003-02-17 Processes for the synthesis of 5’-deoxy-5’ chloroadenosine and 5’-deoxy-5’methylthioadenosine

Publications (1)

Publication Number Publication Date
BR0308091A true BR0308091A (en) 2004-12-21

Family

ID=27789105

Family Applications (1)

Application Number Title Priority Date Filing Date
BR0308091-9A BR0308091A (en) 2002-03-04 2003-02-17 Processes for the synthesis of 5'-deoxy-5'-chloroadenosine and 5'-deoxy-5'-methylthioadenosine

Country Status (20)

Country Link
US (1) US20030181713A1 (en)
EP (1) EP1483279A1 (en)
KR (1) KR20040094761A (en)
CN (1) CN1639182A (en)
AR (1) AR038716A1 (en)
AU (1) AU2003206011A1 (en)
BR (1) BR0308091A (en)
CA (1) CA2477729A1 (en)
GT (1) GT200300047A (en)
HN (1) HN2003000082A (en)
IL (1) IL163778A0 (en)
MX (1) MXPA04008550A (en)
PA (1) PA8567901A1 (en)
PE (1) PE20031002A1 (en)
PL (1) PL370863A1 (en)
RU (1) RU2004126699A (en)
SV (1) SV2004001491A (en)
TW (1) TW200304826A (en)
UY (1) UY27693A1 (en)
WO (1) WO2003074541A1 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2014163150A1 (en) * 2013-04-05 2014-10-09 ライオン株式会社 Composition for internal use

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4373122A (en) * 1981-01-26 1983-02-08 W. H. Brady Co. Capacitance switch
US4454122A (en) * 1981-04-27 1984-06-12 Bioresearch S.R.L. Adenosine derivatives of anti-inflammatory and analgesic activity, and therapeutic compositions which contain them as their active principle
US4373097A (en) * 1981-04-27 1983-02-08 Bioresearch S.R.L. Process for preparing adenosine derivatives of anti-inflammatory and analgesic activity
JPS61171423A (en) * 1985-01-24 1986-08-02 Advance Res & Dev Co Ltd Drug for alleviating dental caries and periodontosis
US6492349B1 (en) * 1993-03-31 2002-12-10 Nutramax Laboratories, Inc. Aminosugar and glycosaminoglycan composition for the treatment and repair of connective tissue
US5872104A (en) * 1994-12-27 1999-02-16 Oridigm Corporation Combinations and methods for reducing antimicrobial resistance

Also Published As

Publication number Publication date
MXPA04008550A (en) 2004-12-06
EP1483279A1 (en) 2004-12-08
CN1639182A (en) 2005-07-13
PE20031002A1 (en) 2003-11-29
HN2003000082A (en) 2004-05-05
SV2004001491A (en) 2004-05-07
RU2004126699A (en) 2005-04-10
PA8567901A1 (en) 2003-11-12
KR20040094761A (en) 2004-11-10
AU2003206011A1 (en) 2003-09-16
CA2477729A1 (en) 2003-09-12
TW200304826A (en) 2003-10-16
AR038716A1 (en) 2005-01-26
UY27693A1 (en) 2003-10-31
GT200300047A (en) 2003-10-10
US20030181713A1 (en) 2003-09-25
WO2003074541A1 (en) 2003-09-12
IL163778A0 (en) 2005-12-18
PL370863A1 (en) 2005-05-30

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Legal Events

Date Code Title Description
B11Y Definitive dismissal - extension of time limit for request of examination expired [chapter 11.1.1 patent gazette]